| Term Name: | heparin cofactor II deficiency |
|---|---|
| Synonyms: | HCF 2 deficiency, HCF II deficiency, THPH10, thrombophilia due to heparin cofactor II deficiency |
| Definition: | A thrombophilia characterized by increased risk of thromboembolism that has_material_basis_in heterozygous mutation in the HCF2 gene on chromosome 22q11.21. |
| Ontology: | Human Disease [DOID:0111901] ( DOID:0111901 ) |